|
注册号: Registration number: |
ChiCTR2600116123 |
|
最近更新日期: Date of Last Refreshed on: |
2026-01-06 08:43:57 |
|
注册时间: Date of Registration: |
2026-01-06 00:00:00 |
|
注册号状态: |
补注册 |
|
Registration Status: |
Retrospective registration |
|
注册题目: |
术中应用艾司洛尔对冠脉病变患者非心脏手术后心血管不良事件的影响:一项单中心、双向队列研究 |
|
Public title: |
The impact of intraoperative esmolol on postoperative cardiovascular adverse events in patients with coronary artery disease undergoing non-cardiac surgery: A single-center, bidirectional cohort study |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
术中应用艾司洛尔对冠脉病变患者非心脏手术后心血管不良事件的影响:一项单中心、双向队列研究 |
|
Scientific title: |
The impact of intraoperative esmolol on postoperative cardiovascular adverse events in patients with coronary artery disease undergoing non-cardiac surgery: A single-center, bidirectional cohort study |
|
研究课题代号(代码): Study subject ID: |
|
|
在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
|
申请注册联系人: |
李松洁 |
研究负责人: |
谷长平 |
|
Applicant: |
Li Songjie |
Study leader: |
Gu Changping |
|
申请注册联系人电话: Applicant telephone: |
+86 156 5135 8117 |
研究负责人电话:
Study leader's |
+86 158 0660 7957 |
|
申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
||
|
申请注册联系人电子邮件: Applicant E-mail: |
lisongjie2000@163.com |
研究负责人电子邮件: Study leader's E-mail: |
jsmggcp@163.com |
|
申请单位网址(自愿提供): Applicant website(voluntary supply): |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
||
|
申请注册联系人通讯地址: |
山东省济南市槐荫区槐村街68号 |
研究负责人通讯地址: |
山东省济南市槐荫区经五纬七路324号 |
|
Applicant address: |
No. 68, Huicun Street, Huayin District, Jinan City, Shandong Province |
Study leader's address: |
No. 324, Jingwu Weixi Road, Huaing District, Jinan City, Shandong Province |
|
申请注册联系人邮政编码: Applicant postcode: |
研究负责人邮政编码: Study leader's postcode: |
||
|
申请人所在单位: |
山东省立医院 |
||
|
Applicant's institution: |
Shandong Provincal Hospital |
||
|
研究负责人所在单位: |
山东省立医院 |
||
|
Affiliation of the Leader: |
Shandong Provincal Hospital |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
省医伦批第(SWYX:NO,2023-559) |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
|
批准本研究的伦理委员会名称: |
山东省立医院涉及人的生物医学研究伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee for Biomedical Research Involving Human Resources of Shandong Provincial Hospital |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2023-11-22 00:00:00 | ||
|
伦理委员会联系人: |
杨爱辉 |
||
|
Contact Name of the ethic committee: |
Yang Aihui |
||
|
伦理委员会联系地址: |
山东省济南市槐荫区经五纬七路324号 |
||
|
Contact Address of the ethic committee: |
No.324 Jingwu Weiqi Road, Huaiyin District, Jinan, Shandong |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 531 6877 6212 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
|
|
研究实施负责(组长)单位: |
山东省立医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Shandong Provincal Hospital |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
山东省济南市槐荫区经五纬七路324号 |
||||||||||||||||||||||
|
Primary sponsor's address: |
No. 324, Jingwu Weixi Road, Huaing District, Jinan City, Shandong Province |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
自筹 |
||||||||||||||||||||||
|
Source(s) of funding: |
self-financing |
||||||||||||||||||||||
|
研究疾病: |
非心脏手术后心血管不良事件 |
||||||||||||||||||||||
|
Target disease: |
cardiovascular adverse events after non-cardiac surgery |
||||||||||||||||||||||
|
研究疾病代码: |
|
||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||
|
研究所处阶段: |
其它 | ||||||||||||||||||||||
|
Study phase: |
N/A |
||||||||||||||||||||||
|
研究设计: |
队列研究 |
||||||||||||||||||||||
|
Study design: |
Cohort study |
||||||||||||||||||||||
|
研究目的: |
评价术中给予艾司洛尔对预防冠脉病变患者接受非心脏手术后心血管不良事件的有效性 |
||||||||||||||||||||||
|
Objectives of Study: |
To evaluate the effectiveness of intraoperative administration of esmolol in preventing adverse cardiovascular events in patients with coronary artery disease after non-cardiac surgery |
||||||||||||||||||||||
|
药物成份或治疗方案详述: |
麻醉诱导、麻醉维持、麻醉苏醒任意过程中静脉推注或泵注艾司洛尔 |
||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
During any of the processes of anesthesia induction, anesthesia maintenance, or anesthesia recovery, esmolol was not intravenously injected or pumped. |
||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||
|
排除标准: |
(1)术前使用β-受体阻滞剂; (2)需禁用或慎用艾司洛尔者:窦性心动过缓患者,病态窦房结综合征、房室传导阻滞、心力衰竭、心源性休克、肺动脉高压、哮喘、慢性阻塞性肺病以及对艾司洛尔过敏等; (3)围手术期因非缺血性疾病(如败血症、肺栓塞、心脏复律)而引起肌钙蛋白升高患者; (4)术前或术后临床资料不全患者。 |
||||||||||||||||||||||
|
Exclusion criteria: |
(1) Use beta-blockers before the operation; (2) Those who need to avoid or use with caution esmolol: patients with sinus bradycardia, sick sinus syndrome, atrioventricular block, heart failure, cardiogenic shock, pulmonary hypertension, asthma, chronic obstructive pulmonary disease, and those allergic to esmolol; (3) Patients with elevated troponin levels during the perioperative period due to non-ischemic diseases (such as sepsis, pulmonary embolism, cardiac cardioversion); (4) Patients with incomplete clinical data before or after the operation. |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2024-11-01 00:00:00至 To 2026-05-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2024-11-01 00:00:00 至 To 2026-05-31 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
正在进行 Recruiting |
年龄范围: Participant age: |
|
||||||
|
性别: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
无 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
None |
||||||||
|
是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
|
盲法: |
无 |
|
Blinding: |
None |
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
是Yes |
|
共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
试验结束后,通过临床试验公共管理平台向公众开放查询;国家生物信息中心 China National center for Bioinformation (https://ngdc.cncb.ac.cn/gsub/)。 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the end of the trial, open access to the public through the public management platform for clinical trials; China National center for Bioinformation (https://ngdc.cncb.ac.cn/gsub/). |
|
数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
病例记录表 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
暂未确定/Not yet |